Examples of using Intravenous administration in English and their translations into Finnish
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Nonafact should be injected into a vein intravenous administration.
Following intravenous administration, plasma concentrations decline in a biphasic or triphasic manner.
Further intravenous administration is not contraindicated unless the reactions reoccur or worsen.
Following intravenous administration, mycophenolate mofetil undergoes rapid and complete metabolism to the active metabolite, MPA.
Intravenous administration should not be protracted over more than 2 hours.
Intravenous administration should not be protracted over more than 2 hours.
Following intravenous administration, naloxone is rapidly distributed distribution half-life~ 4 minutes.
After internal administration or intravenous administration, the desired effect is achieved in 2-5 hours.
Antibodies to omalizumab were detected in some monkeys following repeated subcutaneous or intravenous administration.
It should be used within 6 hours including the one hour infusion intravenous administration.
Reversible cardiotoxic effects were observed in rabbits following intravenous administration of tacrolimus.
Flebogamma DIF is given by injection into your veins intravenous administration.
Reversible cardiotoxic effects were observed in rabbits following intravenous administration of tacrolimus.
Following intravenous administration of Cyanokit, significant binding to plasma proteins
Following intravenous administration teduglutide plasma clearance was approximately 127 ml/hr/kg which is equivalent to the glomerular filtration rate GFR.
Following intravenous administration, the mean volume of distribution was 76± 26 L, and systemic clearance was 147± 47 L/h.
Following intravenous administration, the volume of distribution was about 0.04 to 0.05 L/kg indicating that alirocumab is distributed primarily in the circulatory system.
During the intravenous administration of Nimotop it is very important to follow all the rules of dosing and the method of infusion.
Intravenous administration of fusidic acid and high dose flucloxacillin(infusion of 500 mg
The mean volume of distribution during the terminal phase(Vz) following single intravenous administration ranged from 7.10 to 8.60 litres in plaque psoriasis patients,